Global Patent Index - EP 0983390 A1

EP 0983390 A1 20000308 - INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE

Title (en)

INDIRECT GENOTYPIC METHOD FOR DIAGNOSING TYPE 2 FAMILIAL HEMIPLEGIC MIGRAINE

Title (de)

DIAGNOSTISCHES VERFAHREN ZUR GENOTYPISIERUNG FAMILIÄRER HEMIPLEGISCHER MIGRÄNE VOM TYP 2

Title (fr)

METHODE DE DIAGNOSTIC GENOTYPIQUE INDIRECT DE LA MIGRAINE HEMIPLEGIQUE FAMILIALE DE TYPE 2

Publication

EP 0983390 A1 20000308 (FR)

Application

EP 98929511 A 19980608

Priority

  • FR 9801162 W 19980608
  • FR 9707033 A 19970606

Abstract (en)

[origin: FR2764306A1] The invention concerns an indirect genotypic method for diagnosing type 2 familial hemiplegic migraine in a person, characterised in that it consists in: isolating in said person's DNA the presence of a marker located on the 1a21-q23 chromosome in the locus limited by the D1S2343 and D1S2844 markers, said marker being related with the occurrence of familial hemiplegic migraine in his family.

IPC 1-7

C12Q 1/68

IPC 8 full level

C12N 15/12 (2006.01); C12Q 1/68 (2006.01); C12Q 1/6883 (2018.01)

CPC (source: EP)

C12Q 1/6883 (2013.01); C12Q 2600/156 (2013.01); C12Q 2600/172 (2013.01)

Citation (search report)

See references of WO 9855647A1

Designated contracting state (EPC)

AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

DOCDB simple family (publication)

FR 2764306 A1 19981211; FR 2764306 B1 20010810; CA 2292795 A1 19981210; EP 0983390 A1 20000308; WO 9855647 A1 19981210

DOCDB simple family (application)

FR 9707033 A 19970606; CA 2292795 A 19980608; EP 98929511 A 19980608; FR 9801162 W 19980608